Talk:Alkyl Halide - Revision history

Liuzehui: /* radical reaction (Nora Liu) */ new section

2019-03-10T21:08:29Z

radical reaction (Nora Liu): new section

← Older revision		Revision as of 21:08, 10 March 2019
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	Two step synthesis of Bromobenzene from Aniline using sodium nitrate and CuBr.		Two step synthesis of Bromobenzene from Aniline using sodium nitrate and CuBr.
	[[File:Bromobenzene_synthesis.png\|800px]]		[[File:Bromobenzene_synthesis.png\|800px]]

			== radical reaction (Nora Liu) ==

			[[File: Radical_reaction_(Nora_Liu).png\|600px]]

2019-03-09T01:38:21Z

Synthesis of Bromobenzene from Aniline (Nichole Hannan): new section

← Older revision		Revision as of 01:38, 9 March 2019
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	In this procedure, convert carboxylic acid to acyl chloride with SOCl2. Then reduce the carbonyl carbon so as to remove the carbonyl from the compound with a combination of Sn and HCl.		In this procedure, convert carboxylic acid to acyl chloride with SOCl2. Then reduce the carbonyl carbon so as to remove the carbonyl from the compound with a combination of Sn and HCl.
	[[File:Alkyl Halide Formation.png\|850px]]		[[File:Alkyl Halide Formation.png\|850px]]

			== Synthesis of Bromobenzene from Aniline (Nichole Hannan) ==

			Two step synthesis of Bromobenzene from Aniline using sodium nitrate and CuBr.
			[[File:Bromobenzene_synthesis.png\|800px]]

2019-03-08T19:29:22Z

Alkyl Halide Formation: new section

← Older revision		Revision as of 19:29, 8 March 2019
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	The hydroxyl group attacks the proton on HCl and leaves as water, followed by chloride ion attacking the carbo cation. [[File:1.png]]		The hydroxyl group attacks the proton on HCl and leaves as water, followed by chloride ion attacking the carbo cation. [[File:1.png]]

			== Alkyl Halide Formation ==

			In this procedure, convert carboxylic acid to acyl chloride with SOCl2. Then reduce the carbonyl carbon so as to remove the carbonyl from the compound with a combination of Sn and HCl.
			[[File:Alkyl Halide Formation.png\|850px]]

2019-01-28T06:46:39Z

Synthesis of bromopropane from propanol (Reese Zhu)

← Older revision		Revision as of 06:46, 28 January 2019
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	The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]]		The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]]

	== Synthesis of ~~bromopropane~~ from ~~propanol~~ (~~Reese Zhu~~) ==		== Synthesis of chlorobutane from butanol (Derrick Okine) ==

	The hydroxyl group attacks the proton on ~~HBr~~ and leaves as water, followed by ~~bromide~~ ion attacking the carbo cation. [[File:~~Alkyl_Halide~~.png]]		The hydroxyl group attacks the proton on HCl and leaves as water, followed by chloride ion attacking the carbo cation. [[File:1.png]]

2019-01-28T06:41:36Z

Synthesis of bromopropane from propanol (Reese Zhu)

← Older revision		Revision as of 06:41, 28 January 2019
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	[[Main_Page]]		[[Main_Page]]
	__TOC__		__TOC__

			== Synthesis of bromopropane from propanol (Reese Zhu) ==

			The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]]

	== Synthesis of bromopropane from propanol (Reese Zhu) ==		== Synthesis of bromopropane from propanol (Reese Zhu) ==

	The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]]		The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]]

2019-01-27T20:06:41Z

Synthesis of bromopropane from propanol (Reese Zhu): new section

← Older revision		Revision as of 20:06, 27 January 2019
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	[[Main_Page]]		[[Main_Page]]
	__TOC__		__TOC__

			== Synthesis of bromopropane from propanol (Reese Zhu) ==

			The hydroxyl group attacks the proton on HBr and leaves as water, followed by bromide ion attacking the carbo cation. [[File:Alkyl_Halide.png]]

2019-01-17T19:02:37Z

Cleared out previous entries

← Older revision		Revision as of 19:02, 17 January 2019
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	[[Main_Page]]		[[Main_Page]]
	__TOC__		__TOC__

	~~== Jacob Morsch ==~~

	~~[[File:Alkyl_halide.png\|1100px]]~~

	~~== Acetyl chloride (Imany Noel) ==~~

	~~[[File:Alkyl_Halide.png\|1100px]]~~

	~~A reaction of acetic acid with thionyl chloride to form acetyl chloride.~~

	~~== 2-bromobutane synthesis (Yeaseul Kim) ==~~

	~~[[File: 2-bromobutane_synthesis.png\|1100px]]~~

	~~== Bromoacetone (James Mersch) ==~~

	~~[[File:Bromoacetone (James Mersch).png\|1100px]]~~

	~~== Aryl Halide Formation (Nannan Ji) ==~~

	~~[[File:Reaction2NIS-TFA.png]]~~

	~~== Electrophilic Aromatic Substitution (Suze Jiang) ==~~

	~~[[File:B.png\|150px]]~~

	~~== 2-bromo-2-methylbutane (Sam LaMotte) ==~~

	~~[[File:Wiki_Assignment_2.png\|1100px]]~~

	~~== Pyrrole and Br2 Rxn (Benjamin Lim) ==~~

	~~[[File:O-Chem_2_Wiki.png\|1100px]]~~

	~~== Addtion of methylcholorine to Benzene (Matthew Palmeri) ==~~

	~~[[File:Addtion_of_methylcholorine_to_Benzene.png\|1000px]]~~

	~~== Cyclohexene Bromination ==~~

	~~[[File:Screen Shot 2018-05-15 at 7.46.38 AM.png]]~~

2018-05-15T12:49:13Z

Cyclohexene Bromination

2018-05-15T12:47:48Z

Cyclohexene Bromination: new section

← Older revision		Revision as of 12:47, 15 May 2018
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	[[File:Addtion_of_methylcholorine_to_Benzene.png\|1000px]]		[[File:Addtion_of_methylcholorine_to_Benzene.png\|1000px]]

			== Cyclohexene Bromination ==

			[[File:Screen Shot 2018-05-15 at 7.46.38 AM]]

2018-05-11T21:20:50Z

← Older revision		Revision as of 21:20, 11 May 2018
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	[[File:O-Chem_2_Wiki.png\|1100px]]		[[File:O-Chem_2_Wiki.png\|1100px]]

	== Addtion of methylcholorine to Benzene ==		== Addtion of methylcholorine to Benzene (Matthew Palmeri) ==

	[[File:Addtion_of_methylcholorine_to_Benzene.png\|1000px]]		[[File:Addtion_of_methylcholorine_to_Benzene.png\|1000px]]